(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

Base Information

Chemical Name:(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one
CAS No.:1401338-44-0
Molecular Formula:C₄₀H₄₅NO₄Si₂
Molecular Weight:659.973
Hs Code.:

Synonyms:(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

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Chemical Property of (S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

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Technology Process of (S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

There total 3 articles about (S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

: 76-86-8
Triphenylsilyl chloride

: 376585-98-7
(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-hydroxy-2-methylpent-4-ynoyl]oxazolidin-2-one

: 1401338-44-0
(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide;
DOI:10.1039/c2ob26185e

Reference yield:

: 90083-19-5
3-(tert-butyldimethylsilyl)-2-propynal

: 1401338-44-0
(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine; di-n-butylboryl trifluoromethanesulfonate / dichloromethane / 1 h / -78 °C

1.2: -78 - 0 °C

2.1: 1H-imidazole / N,N-dimethyl-formamide

With 1H-imidazole; di-n-butylboryl trifluoromethanesulfonate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c2ob26185e

Reference yield:

: 86318-61-8
(tert-butyldimethylsilyl)acetylene

: 1401338-44-0
(S)-9-benzyl-3-[(2S,3S)-5-(tert-butyldimethylsilyl)-3-(triphenylsilyloxy)-2-methylpent-4-ynoyl]oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran / 0.33 h / 0 °C

1.2: 0 °C / Reflux

2.1: triethylamine; di-n-butylboryl trifluoromethanesulfonate / dichloromethane / 1 h / -78 °C

2.2: -78 - 0 °C

3.1: 1H-imidazole / N,N-dimethyl-formamide

With 1H-imidazole; n-butyllithium; di-n-butylboryl trifluoromethanesulfonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c2ob26185e